• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

血管性血友病因子,血流中的绝地武士。

von Willebrand factor, Jedi knight of the bloodstream.

作者信息

Springer Timothy A

机构信息

Program in Cellular and Molecular Medicine and Division of Hematology, Department of Medicine, Boston Children's Hospital, and Department of Biological Chemistry and Pharmacology, Harvard Medical School, Boston, MA.

出版信息

Blood. 2014 Aug 28;124(9):1412-25. doi: 10.1182/blood-2014-05-378638. Epub 2014 Jun 13.

DOI:10.1182/blood-2014-05-378638
PMID:24928861
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4148764/
Abstract

When blood vessels are cut, the forces in the bloodstream increase and change character. The dark side of these forces causes hemorrhage and death. However, von Willebrand factor (VWF), with help from our circulatory system and platelets, harnesses the same forces to form a hemostatic plug. Force and VWF function are so closely intertwined that, like members of the Jedi Order in the movie Star Wars who learn to use "the Force" to do good, VWF may be considered the Jedi knight of the bloodstream. The long length of VWF enables responsiveness to flow. The shape of VWF is predicted to alter from irregularly coiled to extended thread-like in the transition from shear to elongational flow at sites of hemostasis and thrombosis. Elongational force propagated through the length of VWF in its thread-like shape exposes its monomers for multimeric binding to platelets and subendothelium and likely also increases affinity of the A1 domain for platelets. Specialized domains concatenate and compact VWF during biosynthesis. A2 domain unfolding by hydrodynamic force enables postsecretion regulation of VWF length. Mutations in VWF in von Willebrand disease contribute to and are illuminated by VWF biology. I attempt to integrate classic studies on the physiology of hemostatic plug formation into modern molecular understanding, and point out what remains to be learned.

摘要

血管被割破时,血流中的力会增加并改变性质。这些力的负面影响会导致出血和死亡。然而,在我们的循环系统和血小板的帮助下,血管性血友病因子(VWF)利用同样的力形成止血栓。力与VWF的功能紧密相连,就像电影《星球大战》中学会运用“原力”行善的绝地武士团成员一样,VWF可被视为血流中的绝地骑士。VWF的长链使其能够对血流做出反应。预计在止血和血栓形成部位,从剪切流转变为拉伸流时,VWF的形状会从不规则盘绕变为伸展的丝状。通过其丝状形状的VWF长度传播的拉伸力会暴露其单体,以便与血小板和内皮下层进行多聚体结合,并且可能还会增加A1结构域对血小板的亲和力。在生物合成过程中,特殊结构域将VWF连接并压缩在一起。水动力使A2结构域展开,从而实现VWF长度的分泌后调节。血管性血友病中VWF的突变有助于VWF生物学研究,同时也从VWF生物学研究中得到阐释。我试图将关于止血栓形成生理学的经典研究与现代分子理解相结合,并指出仍有待了解的内容。

相似文献

1
von Willebrand factor, Jedi knight of the bloodstream.血管性血友病因子,血流中的绝地武士。
Blood. 2014 Aug 28;124(9):1412-25. doi: 10.1182/blood-2014-05-378638. Epub 2014 Jun 13.
2
Biophysical approaches promote advances in the understanding of von Willebrand factor processing and function.生物物理方法推动了对血管性血友病因子加工和功能理解的进展。
Adv Biol Regul. 2017 Jan;63:81-91. doi: 10.1016/j.jbior.2016.09.010. Epub 2016 Sep 28.
3
Molecular modeling of ligand and mutation sites of the type A domains of human von Willebrand factor and their relevance to von Willebrand's disease.人血管性血友病因子A结构域配体与突变位点的分子建模及其与血管性血友病的相关性
Blood. 1998 Mar 15;91(6):2032-44.
4
[von Willebrand factor and von Willebrand disease].[血管性血友病因子与血管性血友病]
Rinsho Ketsueki. 2016;57(10):2113-2123. doi: 10.11406/rinketsu.57.2113.
5
von Willebrand factor, von Willebrand factor-cleaving protease, and shear stress.血管性血友病因子、血管性血友病因子裂解蛋白酶与剪切应力。
Cardiovasc Hematol Agents Med Chem. 2007 Oct;5(4):305-10. doi: 10.2174/187152507782109863.
6
Mutual A domain interactions in the force sensing protein von Willebrand factor.力传感蛋白血管性血友病因子中的相互A结构域相互作用。
J Struct Biol. 2017 Jan;197(1):57-64. doi: 10.1016/j.jsb.2016.04.012. Epub 2016 Apr 23.
7
Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets.2M型:密尔沃基-1型血管性血友病:血管性血友病因子A1结构域的Cys509-Cys695环内的框内缺失导致血管性血友病因子与血小板的结合缺陷。
Blood. 1996 Oct 1;88(7):2559-68.
8
Functional property of von Willebrand factor under flowing blood.血流状态下血管性血友病因子的功能特性
Int J Hematol. 2002 Jan;75(1):19-24. doi: 10.1007/BF02981974.
9
Mechanoenzymatic cleavage of the ultralarge vascular protein von Willebrand factor.超大型血管蛋白血管性血友病因子的机械酶解作用
Science. 2009 Jun 5;324(5932):1330-4. doi: 10.1126/science.1170905.
10
Unfolding the A2 domain of von Willebrand factor with the optical trap.利用光阱展开 von Willebrand 因子的 A2 结构域。
Biophys J. 2010 Apr 21;98(8):1685-93. doi: 10.1016/j.bpj.2009.12.4324.

引用本文的文献

1
Constitutive interaction between neutrophils and von Willebrand factor in peripheral blood.外周血中中性粒细胞与血管性血友病因子之间的组成性相互作用。
Sci Rep. 2025 Jul 10;15(1):24895. doi: 10.1038/s41598-025-10321-6.
2
Cryo-EM structure of native honey bee vitellogenin.天然蜜蜂卵黄原蛋白的冷冻电镜结构
Nat Commun. 2025 Jul 1;16(1):5736. doi: 10.1038/s41467-025-58575-y.
3
Irradiation with 265-nm Ultraviolet Light-Emitting Diodes to Plasma: Alterations of Hemostatic Parameters and von Willebrand Factor.用265纳米紫外发光二极管照射血浆:止血参数和血管性血友病因子的改变。
Transfus Med Hemother. 2025 May 26:1-11. doi: 10.1159/000546169.
4
Genetic analysis using long-read sequencing to overcome the difficulties in gene.使用长读长测序进行基因分析以克服基因研究中的困难。
Res Pract Thromb Haemost. 2025 May 17;9(4):102888. doi: 10.1016/j.rpth.2025.102888. eCollection 2025 May.
5
A direct computational assessment of vinculin-actin unbinding kinetics reveals catch-bonding behavior.对纽蛋白-肌动蛋白解离动力学的直接计算评估揭示了捕获键合行为。
Proc Natl Acad Sci U S A. 2025 May 27;122(21):e2425982122. doi: 10.1073/pnas.2425982122. Epub 2025 May 21.
6
Contrasting Effects of Platelet GPVI Deletion Versus Syk Inhibition on Mouse Jugular Vein Puncture Wound Structure.血小板糖蛋白VI缺失与脾酪氨酸激酶抑制对小鼠颈静脉穿刺伤口结构的对比作用
Int J Mol Sci. 2025 May 1;26(9):4294. doi: 10.3390/ijms26094294.
7
In the flow, how fluid dynamics shapes amyloid formation.在流动过程中,流体动力学如何塑造淀粉样蛋白的形成。
Proc Natl Acad Sci U S A. 2025 Apr 22;122(16):e2504573122. doi: 10.1073/pnas.2504573122. Epub 2025 Apr 15.
8
Dynamics of a von Willebrand Factor A1 Autoinhibitory Module with O-Linked Glycans and Its Roles in Regulation of GPIbα Binding.具有O-连接聚糖的血管性血友病因子A1自抑制模块的动力学及其在调节糖蛋白Ibα结合中的作用。
J Phys Chem B. 2025 Apr 17;129(15):3796-3806. doi: 10.1021/acs.jpcb.5c00925. Epub 2025 Apr 4.
9
RalB uncoupling from exocyst is required for endothelial Weibel-Palade body exocytosis.内皮细胞Weibel-Palade小体胞吐作用需要RalB与外吐复合体解偶联。
Mol Biol Cell. 2025 May 1;36(5):ar62. doi: 10.1091/mbc.E24-11-0493. Epub 2025 Apr 2.
10
MUC5AC filaments illuminate the structural diversification of respiratory and intestinal mucins.MUC5AC细丝揭示了呼吸道和肠道粘蛋白的结构多样性。
Proc Natl Acad Sci U S A. 2025 Mar 11;122(10):e2419717122. doi: 10.1073/pnas.2419717122. Epub 2025 Mar 4.

本文引用的文献

1
Expression of a structurally constrained von Willebrand factor variant triggers acute thrombotic thrombocytopenic purpura in mice.结构受限的血管性血友病因子变异体的表达可引发小鼠急性血栓性血小板减少性紫癜。
Blood. 2014 May 22;123(21):3344-53. doi: 10.1182/blood-2013-10-531392. Epub 2014 Apr 8.
2
Solution structure of the major factor VIII binding region on von Willebrand factor.血管性血友病因子上主要凝血因子VIII结合区域的溶液结构
Blood. 2014 Jun 26;123(26):4143-51. doi: 10.1182/blood-2013-07-517086. Epub 2014 Apr 3.
3
Plasmin cleavage of von Willebrand factor as an emergency bypass for ADAMTS13 deficiency in thrombotic microangiopathy.纤维蛋白溶酶对血管性血友病因子的裂解作用可作为血栓性微血管病中 ADAMTS13 缺乏症的紧急旁路。
Circulation. 2014 Mar 25;129(12):1320-31. doi: 10.1161/CIRCULATIONAHA.113.006727. Epub 2014 Jan 21.
4
The O-linked glycans of human von Willebrand factor modulate its interaction with ADAMTS-13.人血管性血友病因子的 O-连接聚糖调节其与 ADAMTS-13 的相互作用。
J Thromb Haemost. 2014 Jan;12(1):54-61. doi: 10.1111/jth.12451.
5
Highly reinforced structure of a C-terminal dimerization domain in von Willebrand factor.血管性血友病因子 C 末端二聚化结构域的高强化结构。
Blood. 2014 Mar 20;123(12):1785-93. doi: 10.1182/blood-2013-11-523639. Epub 2014 Jan 6.
6
Structural basis of regulation of von Willebrand factor binding to glycoprotein Ib.血管性血友病因子与糖蛋白 Ib 结合调节的结构基础。
J Biol Chem. 2014 Feb 28;289(9):5565-79. doi: 10.1074/jbc.M113.511220. Epub 2014 Jan 3.
7
Von Willebrand factor: form for function.血管性血友病因子:形式决定功能。
Semin Thromb Hemost. 2014 Feb;40(1):17-27. doi: 10.1055/s-0033-1363155. Epub 2013 Dec 13.
8
Characterisation of Weibel-Palade body fusion by amperometry in endothelial cells reveals fusion pore dynamics and the effect of cholesterol on exocytosis.通过在血管内皮细胞中安培法对 Weibel-Palade 体融合进行表征,揭示了融合孔动力学和胆固醇对胞吐作用的影响。
J Cell Sci. 2013 Dec 1;126(Pt 23):5490-9. doi: 10.1242/jcs.138438. Epub 2013 Oct 14.
9
The N-terminal flanking region of the A1 domain regulates the force-dependent binding of von Willebrand factor to platelet glycoprotein Ibα.A1 结构域 N 端侧翼区调节血管性血友病因子与血小板糖蛋白 Ibα 之间的力依赖性结合。
J Biol Chem. 2013 Nov 8;288(45):32289-32301. doi: 10.1074/jbc.M113.504001. Epub 2013 Sep 23.
10
Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia.加速血管性血友病因子/血小板复合物在巨噬细胞中的摄取导致 2B 型血管性血友病相关血小板减少症。
Blood. 2013 Oct 17;122(16):2893-902. doi: 10.1182/blood-2013-03-493312. Epub 2013 Aug 14.